Annotation Detail
Information
- Associated Genes
- EYS
- Associated Variants
-
EYS p.Gly2598Asp (p.G2598D)
(
ENST00000370621.7,
ENST00000503581.6 )
EYS p.Gly2598Asp (p.G2598D) ( ENST00000370621.7, ENST00000503581.6 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_001142800.2(EYS):c.7793G>A (p.Gly2598Asp) AND not specified
- ClinVar Allele ID
- 152829
- ClinVar RefSeq Alternation Syntax
- NM_001292009.2:c.7793G>A
- ClinVar RefSeq Alternation Syntax
- NM_001142800.2:c.7793G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-07-27
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003323413
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs